Package 50090-4236-0

Brand: atomoxetine hydrochloride

Generic: atomoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4236-0
Digits Only 5009042360
Product NDC 50090-4236
Description

30 CAPSULE in 1 BOTTLE (50090-4236-0)

Marketing

Marketing Status
Marketed Since 2019-03-29
Brand atomoxetine hydrochloride
Generic atomoxetine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d1a130e7-3cee-40cf-a4c6-cb3893304987", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["19b10860-aa08-4480-816c-c207819e5f9e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-4236-0)", "package_ndc": "50090-4236-0", "marketing_start_date": "20190329"}], "brand_name": "Atomoxetine Hydrochloride", "product_id": "50090-4236_d1a130e7-3cee-40cf-a4c6-cb3893304987", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-4236", "generic_name": "atomoxetine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine Hydrochloride", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078983", "marketing_category": "ANDA", "marketing_start_date": "20180521", "listing_expiration_date": "20261231"}